Novel regiochemistry in the aqueous singlet oxygen ene reaction of carboxylic acid salts: A comparison of substrate structure

被引：0

作者：

Stensaas, KL ^{[1
]}

Bajaj, A ^{[1
]}

Al-Turk, A ^{[1
]}

机构：

[1] Millsaps Coll, Dept Chem, Jackson, MS 39210 USA

来源：

ABSTRACTS OF PAPERS OF THE AMERICAN CHEMICAL SOCIETY | 2003年 / 225卷

关键词：

D O I：

暂无

中图分类号：

O6 [化学];

学科分类号：

0703 ;

摘要：

571-ORGN

引用

页码：U393 / U393

页数：1

共 24 条

[1] Novel regiochemistry in the aqueous singlet oxygen ene reactions of carboxylic acid salts: a comparison of substrate structure
Stensaas, KL
Bajaj, A
Al-Turk, A
TETRAHEDRON LETTERS, 2005, 46 (04) : 715 - 718
[2] Singlet oxygen ene reaction of tiglic acid utilizing an aqueous solvent.
Stensaas, KL
Means, BC
ABSTRACTS OF PAPERS OF THE AMERICAN CHEMICAL SOCIETY, 1999, 218 : U96 - U96
[3] Aqueous solvents dictate the regiochemistry in the photooxidations of α,β-unsaturated carboxylic acid salts
Stensaas, KL
Bajaj, A
SYNTHESIS-STUTTGART, 2005, (15): : 2623 - 2624
[4] Novel solvent hydrogen-bonding effects in the singlet oxygen ene reaction:: a comparison of α,β-unsaturated esters and acids
Stensaas, KL
Payne, JA
Ivancic, AN
Bajaj, A
TETRAHEDRON LETTERS, 2002, 43 (01) : 25 - 27
[5] An experimental and computational study on the reactivity and regioselectivity for the nitrosoarene ene reaction: Comparison with triazolinedione and singlet oxygen
Adam, W
Bottke, N
Engels, B
Krebs, O
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2001, 123 (23) : 5542 - 5548
[6] Comparison of the aqueous solvent effects on the singlet oxygen ene reactions of angelic acid, 2,3-dimethyl-2-butenoic acid and their salt derivatives.
Stensaas, KL
Payne, JA
Ivancic, AN
Bajaj, A
ABSTRACTS OF PAPERS OF THE AMERICAN CHEMICAL SOCIETY, 2002, 224 : U188 - U189
[7] Steric and conformational control of the regioselectivities in the ene reaction with trisubstituted cycloalkenes: Comparison of the enophiles singlet oxygen, triazolinedione, and nitrosoarene
Adam, W
Bottke, N
Krebs, O
ORGANIC LETTERS, 2000, 2 (21) : 3293 - 3296
[8] Novel diastereoselective allene formation by an ene reaction of significantly twisted 1,3-dienes with singlet oxygen
Mori, H
Matsuo, T
Yamashita, K
Katsumura, S
TETRAHEDRON LETTERS, 1999, 40 (35) : 6461 - 6464
[9] Diastereoselective singlet oxygen ene reaction (Schenck reaction) and diastereoselective epoxidations of heteroatom-substituted acyclic chiral olefins: A mechanistic comparison
Adam, W
Brunker, HG
Kumar, AS
Peters, EM
Peters, K
Schneider, U
vonSchnering, HG
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1996, 118 (08) : 1899 - 1905
[10] The new skew and the established cis and gem regioselectivities in the ene reaction of trisubstituted olefins:: Comparison of the singlet oxygen, triazolinedione, and nitrosoarene enophiles
Adam, W
Bottke, N
Krebs, O
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2000, 122 (28) : 6791 - 6792

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